Related gene-specific medical variations for Gene (Select 8740) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2570209	NM_001376887.1(TNFSF14):c.92A>G (p.Gln31Arg)	LOC130063326, TNFSF14 (Q31R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2255103	NM_001376887.1(TNFSF14):c.134T>C (p.Leu45Ser)	LOC130063326, TNFSF14 (L45S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance